Hoerndli Frederic, David Della C, Götz Jürgen
Division of Psychiatry Research, University of Zurich, 8008 Zurich, Switzerland.
Prog Neurobiol. 2005 Jun;76(3):169-88. doi: 10.1016/j.pneurobio.2005.07.002.
The transcriptomic and proteomic techniques presented in part I (Functional Genomics meets neurodegenerative disorders. Part I: transcriptomic and proteomic technology) of this back-to-back review have been applied to a range of neurodegenerative disorders, including Huntington's disease (HD), Prion diseases (PrD), Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis (ALS), Alzheimer's disease (AD), frontotemporal dementia (FTD) and Parkinson's disease (PD). Samples have been derived either from human brain and cerebrospinal fluid, tissue culture cells or brains and spinal cord of experimental animal models. With the availability of huge data sets it will firstly be a major challenge to extract meaningful information and secondly, not to obtain contradicting results when data are collected in parallel from the same source of biological specimen using different techniques. Reliability of the data highly depends on proper normalization and validation both of which are discussed together with an outlook on developments that can be anticipated in the future and are expected to fuel the field. The new insight undoubtedly will lead to a redefinition and subdivision of disease entities based on biochemical criteria rather than the clinical presentation. This will have important implications for treatment strategies.
在这篇背靠背综述的第一部分(《功能基因组学与神经退行性疾病。第一部分:转录组学和蛋白质组学技术》)中介绍的转录组学和蛋白质组学技术已应用于一系列神经退行性疾病,包括亨廷顿舞蹈病(HD)、朊病毒病(PrD)、克雅氏病、肌萎缩侧索硬化症(ALS)、阿尔茨海默病(AD)、额颞叶痴呆(FTD)和帕金森病(PD)。样本来源于人脑和脑脊液、组织培养细胞或实验动物模型的脑和脊髓。随着大量数据集的可得性,首先,提取有意义的信息将是一项重大挑战;其次,当使用不同技术从同一生物样本来源并行收集数据时,要避免获得相互矛盾的结果。数据的可靠性高度依赖于适当的标准化和验证,本文将对这两者进行讨论,并展望未来可预期的发展,这些发展有望推动该领域的进步。新的见解无疑将导致基于生化标准而非临床表现对疾病实体进行重新定义和细分。这将对治疗策略产生重要影响。